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4yqf

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m (Protected "4yqf" [edit=sysop:move=sysop])
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'''Unreleased structure'''
 
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The entry 4yqf is ON HOLD until Mar 13 2017
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==GTPase domain of Human Septin 9==
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<StructureSection load='4yqf' size='340' side='right'caption='[[4yqf]], [[Resolution|resolution]] 2.73&Aring;' scene=''>
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Authors: Matos, S.O., Leonardo, D.A., Macedo, J.N., Pereira, H.M., Araujo, A.P.U., Garratt, R.C.
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== Structural highlights ==
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<table><tr><td colspan='2'>[[4yqf]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4YQF OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4YQF FirstGlance]. <br>
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Description: GTPase domain of Human Septin 9
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.73&#8491;</td></tr>
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[[Category: Unreleased Structures]]
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=GDP:GUANOSINE-5-DIPHOSPHATE'>GDP</scene>, <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene></td></tr>
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[[Category: Garratt, R.C]]
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=4yqf FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4yqf OCA], [https://pdbe.org/4yqf PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4yqf RCSB], [https://www.ebi.ac.uk/pdbsum/4yqf PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4yqf ProSAT]</span></td></tr>
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[[Category: Pereira, H.M]]
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</table>
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[[Category: Araujo, A.P.U]]
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== Disease ==
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[[Category: Leonardo, D.A]]
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[https://www.uniprot.org/uniprot/SEPT9_HUMAN SEPT9_HUMAN] Neuralgic amyotrophy. A chromosomal aberration involving SEPT9/MSF is found in therapy-related acute myeloid leukemia (t-AML). Translocation t(11;17)(q23;q25) with KMT2A/MLL1.<ref>PMID:10339604</ref> The disease is caused by mutations affecting the gene represented in this entry.
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[[Category: Macedo, J.N]]
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== Function ==
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[[Category: Matos, S.O]]
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[https://www.uniprot.org/uniprot/SEPT9_HUMAN SEPT9_HUMAN] Filament-forming cytoskeletal GTPase (By similarity). May play a role in cytokinesis (Potential). May play a role in the internalization of 2 intracellular microbial pathogens, Listeria monocytogenes and Shigella flexneri.
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== References ==
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<references/>
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__TOC__
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</StructureSection>
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[[Category: Homo sapiens]]
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[[Category: Large Structures]]
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[[Category: Araujo APU]]
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[[Category: Garratt RC]]
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[[Category: Leonardo DA]]
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[[Category: Macedo JN]]
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[[Category: Matos SO]]
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[[Category: Pereira HM]]

Current revision

GTPase domain of Human Septin 9

PDB ID 4yqf

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